Title of article :
Chromosome Duplication (14q) and The Genotype Phenotype Correlation
Author/Authors :
Sadr-Nabavi، Ariane نويسنده Department of Human Genetics, Mashhad University of Medical Sciences, Mashhad, Iran Sadr-Nabavi, Ariane , Saeidi، Morteza نويسنده Department of Neurology, Mashhad University of Medical Sciences, Ghaem hospital, Mashhad, Iran ,
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2014
Abstract :
The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number
or structure of chromosome 14 can have a variety of effects, such as delayed growth and
development, and distinctive facial features. The human chromosome 14 plays an important
role in imprinting events importunes of a structural rearrangement is specifically when
a phenotype is caused by imprinting, whereby the interpretation of genotype-phenotype
correlation becomes extremely difficult. In this study, we examined a 3 year-old mentally
impaired girl with unusual facial features. G-banding showed terminal duplication of chromosome
14 in the karyotype of the patient. In this particular case, we explained a phenotype
genotype correlation in a patient with a dup (14) rearrangement, thus emphasizing the
importance of prenatal diagnosis for pregnancies with an abnormal nuchal translucency.
Journal title :
International Journal of Fertility and Sterility
Journal title :
International Journal of Fertility and Sterility